Hereditary Late-Onset Parkinson Disease (LOPD)

Alias:
Autosomal Dominant Late-Onset Parkinson Disease
Hereditary Late Onset Parkinson Disease
Lopd
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hereditary Late-Onset Parkinson Disease, also known as autosomal dominant late-onset parkinson disease, is related to glucosidase acid-1,4-alpha deficiency and glycogen storage disease ii. An important gene associated with Hereditary Late-Onset Parkinson Disease is DNAJC13 (DnaJ Heat Shock Protein Family (Hsp40) Member C13), and among its related pathways/superpathways are Parkinson's disease pathway and Involvement of -secretase in neurodegenerative diseases. The drugs Temsirolimus and Acetaminophen have been mentioned in the context of this disorder. Affiliated tissues include tongue and subthalamic nucleus, and related phenotypes are parkinsonism and diplopia
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
12
177
75

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top